Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 5 |
GO:0110165 | cellular anatomical entity | 1 | 5 |
Related structures:
AlphaFold database: A4HQD4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 112 | 114 | PF00675 | 0.440 |
CLV_NRD_NRD_1 | 310 | 312 | PF00675 | 0.418 |
CLV_NRD_NRD_1 | 337 | 339 | PF00675 | 0.416 |
CLV_PCSK_KEX2_1 | 112 | 114 | PF00082 | 0.465 |
CLV_PCSK_KEX2_1 | 337 | 339 | PF00082 | 0.323 |
CLV_PCSK_SKI1_1 | 315 | 319 | PF00082 | 0.356 |
CLV_PCSK_SKI1_1 | 337 | 341 | PF00082 | 0.301 |
CLV_TASPASE1 | 58 | 64 | PF01112 | 0.639 |
DEG_SPOP_SBC_1 | 165 | 169 | PF00917 | 0.720 |
DEG_SPOP_SBC_1 | 254 | 258 | PF00917 | 0.641 |
DEG_SPOP_SBC_1 | 275 | 279 | PF00917 | 0.771 |
DOC_CDC14_PxL_1 | 351 | 359 | PF14671 | 0.364 |
DOC_CYCLIN_yCln2_LP_2 | 14 | 20 | PF00134 | 0.564 |
DOC_PP4_FxxP_1 | 352 | 355 | PF00568 | 0.431 |
DOC_USP7_MATH_1 | 165 | 169 | PF00917 | 0.763 |
DOC_USP7_MATH_1 | 229 | 233 | PF00917 | 0.623 |
DOC_USP7_MATH_1 | 254 | 258 | PF00917 | 0.635 |
DOC_USP7_MATH_1 | 275 | 279 | PF00917 | 0.804 |
DOC_USP7_MATH_1 | 4 | 8 | PF00917 | 0.608 |
DOC_WW_Pin1_4 | 155 | 160 | PF00397 | 0.717 |
DOC_WW_Pin1_4 | 268 | 273 | PF00397 | 0.701 |
LIG_14-3-3_CanoR_1 | 295 | 303 | PF00244 | 0.516 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.617 |
LIG_BIR_III_2 | 288 | 292 | PF00653 | 0.563 |
LIG_deltaCOP1_diTrp_1 | 101 | 107 | PF00928 | 0.623 |
LIG_FHA_1 | 256 | 262 | PF00498 | 0.689 |
LIG_FHA_1 | 351 | 357 | PF00498 | 0.231 |
LIG_FHA_1 | 40 | 46 | PF00498 | 0.626 |
LIG_FHA_2 | 115 | 121 | PF00498 | 0.674 |
LIG_FHA_2 | 180 | 186 | PF00498 | 0.627 |
LIG_FHA_2 | 65 | 71 | PF00498 | 0.579 |
LIG_FHA_2 | 8 | 14 | PF00498 | 0.564 |
LIG_LIR_Gen_1 | 104 | 115 | PF02991 | 0.571 |
LIG_LIR_Nem_3 | 101 | 106 | PF02991 | 0.576 |
LIG_LIR_Nem_3 | 149 | 155 | PF02991 | 0.748 |
LIG_LIR_Nem_3 | 298 | 303 | PF02991 | 0.497 |
LIG_LYPXL_SIV_4 | 72 | 80 | PF13949 | 0.519 |
LIG_NRBOX | 335 | 341 | PF00104 | 0.499 |
LIG_PDZ_Class_2 | 359 | 364 | PF00595 | 0.312 |
LIG_PTB_Apo_2 | 28 | 35 | PF02174 | 0.512 |
LIG_PTB_Phospho_1 | 28 | 34 | PF10480 | 0.511 |
LIG_SH2_CRK | 307 | 311 | PF00017 | 0.507 |
LIG_SH2_CRK | 34 | 38 | PF00017 | 0.528 |
LIG_SH2_GRB2like | 319 | 322 | PF00017 | 0.444 |
LIG_SH2_STAP1 | 293 | 297 | PF00017 | 0.592 |
LIG_SH2_STAP1 | 73 | 77 | PF00017 | 0.527 |
LIG_SH2_STAT5 | 307 | 310 | PF00017 | 0.497 |
LIG_SH2_STAT5 | 319 | 322 | PF00017 | 0.502 |
LIG_SH2_STAT5 | 345 | 348 | PF00017 | 0.317 |
LIG_SH2_STAT5 | 97 | 100 | PF00017 | 0.529 |
LIG_SH3_3 | 207 | 213 | PF00018 | 0.636 |
LIG_SUMO_SIM_anti_2 | 89 | 96 | PF11976 | 0.459 |
LIG_TRAF2_1 | 136 | 139 | PF00917 | 0.634 |
LIG_TYR_ITIM | 305 | 310 | PF00017 | 0.486 |
LIG_UBA3_1 | 94 | 100 | PF00899 | 0.576 |
MOD_CK1_1 | 127 | 133 | PF00069 | 0.641 |
MOD_CK1_1 | 164 | 170 | PF00069 | 0.632 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.605 |
MOD_CK1_1 | 239 | 245 | PF00069 | 0.695 |
MOD_CK1_1 | 246 | 252 | PF00069 | 0.701 |
MOD_CK1_1 | 268 | 274 | PF00069 | 0.753 |
MOD_CK1_1 | 83 | 89 | PF00069 | 0.561 |
MOD_CK2_1 | 132 | 138 | PF00069 | 0.638 |
MOD_CK2_1 | 16 | 22 | PF00069 | 0.564 |
MOD_CK2_1 | 179 | 185 | PF00069 | 0.624 |
MOD_CK2_1 | 281 | 287 | PF00069 | 0.714 |
MOD_CK2_1 | 64 | 70 | PF00069 | 0.589 |
MOD_CK2_1 | 83 | 89 | PF00069 | 0.486 |
MOD_GlcNHglycan | 134 | 137 | PF01048 | 0.440 |
MOD_GlcNHglycan | 155 | 158 | PF01048 | 0.484 |
MOD_GlcNHglycan | 163 | 166 | PF01048 | 0.443 |
MOD_GlcNHglycan | 168 | 171 | PF01048 | 0.541 |
MOD_GlcNHglycan | 188 | 191 | PF01048 | 0.462 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.481 |
MOD_GlcNHglycan | 201 | 204 | PF01048 | 0.515 |
MOD_GlcNHglycan | 218 | 221 | PF01048 | 0.437 |
MOD_GlcNHglycan | 231 | 234 | PF01048 | 0.520 |
MOD_GlcNHglycan | 238 | 241 | PF01048 | 0.477 |
MOD_GlcNHglycan | 248 | 251 | PF01048 | 0.451 |
MOD_GSK3_1 | 153 | 160 | PF00069 | 0.631 |
MOD_GSK3_1 | 16 | 23 | PF00069 | 0.520 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.635 |
MOD_GSK3_1 | 186 | 193 | PF00069 | 0.770 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.661 |
MOD_GSK3_1 | 239 | 246 | PF00069 | 0.648 |
MOD_GSK3_1 | 249 | 256 | PF00069 | 0.756 |
MOD_GSK3_1 | 267 | 274 | PF00069 | 0.743 |
MOD_GSK3_1 | 276 | 283 | PF00069 | 0.693 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.642 |
MOD_GSK3_1 | 64 | 71 | PF00069 | 0.706 |
MOD_NEK2_1 | 132 | 137 | PF00069 | 0.637 |
MOD_NEK2_1 | 153 | 158 | PF00069 | 0.640 |
MOD_NEK2_1 | 199 | 204 | PF00069 | 0.692 |
MOD_NEK2_1 | 20 | 25 | PF00069 | 0.509 |
MOD_NEK2_1 | 255 | 260 | PF00069 | 0.707 |
MOD_NEK2_1 | 265 | 270 | PF00069 | 0.672 |
MOD_NEK2_1 | 35 | 40 | PF00069 | 0.627 |
MOD_NEK2_1 | 350 | 355 | PF00069 | 0.366 |
MOD_PIKK_1 | 255 | 261 | PF00454 | 0.698 |
MOD_PKA_2 | 199 | 205 | PF00069 | 0.745 |
MOD_PKA_2 | 280 | 286 | PF00069 | 0.645 |
MOD_Plk_1 | 68 | 74 | PF00069 | 0.605 |
MOD_Plk_1 | 83 | 89 | PF00069 | 0.469 |
MOD_Plk_2-3 | 16 | 22 | PF00069 | 0.564 |
MOD_Plk_4 | 106 | 112 | PF00069 | 0.548 |
MOD_Plk_4 | 16 | 22 | PF00069 | 0.562 |
MOD_Plk_4 | 193 | 199 | PF00069 | 0.630 |
MOD_Plk_4 | 220 | 226 | PF00069 | 0.663 |
MOD_Plk_4 | 47 | 53 | PF00069 | 0.488 |
MOD_Plk_4 | 83 | 89 | PF00069 | 0.583 |
MOD_ProDKin_1 | 155 | 161 | PF00069 | 0.718 |
MOD_ProDKin_1 | 268 | 274 | PF00069 | 0.703 |
MOD_SUMO_rev_2 | 156 | 165 | PF00179 | 0.632 |
TRG_DiLeu_BaEn_1 | 16 | 21 | PF01217 | 0.502 |
TRG_DiLeu_BaEn_1 | 331 | 336 | PF01217 | 0.471 |
TRG_DiLeu_BaEn_1 | 89 | 94 | PF01217 | 0.571 |
TRG_DiLeu_BaEn_4 | 331 | 337 | PF01217 | 0.568 |
TRG_DiLeu_BaLyEn_6 | 322 | 327 | PF01217 | 0.551 |
TRG_DiLeu_BaLyEn_6 | 335 | 340 | PF01217 | 0.487 |
TRG_DiLeu_BaLyEn_6 | 352 | 357 | PF01217 | 0.312 |
TRG_ENDOCYTIC_2 | 293 | 296 | PF00928 | 0.578 |
TRG_ENDOCYTIC_2 | 300 | 303 | PF00928 | 0.466 |
TRG_ENDOCYTIC_2 | 307 | 310 | PF00928 | 0.404 |
TRG_ENDOCYTIC_2 | 34 | 37 | PF00928 | 0.558 |
TRG_ER_diArg_1 | 111 | 113 | PF00400 | 0.662 |
TRG_ER_diArg_1 | 336 | 338 | PF00400 | 0.615 |
TRG_NES_CRM1_1 | 46 | 60 | PF08389 | 0.558 |
TRG_Pf-PMV_PEXEL_1 | 85 | 89 | PF00026 | 0.269 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I247 | Leptomonas seymouri | 37% | 100% |
A0A3S7XC14 | Leishmania donovani | 62% | 100% |
A4IE26 | Leishmania infantum | 62% | 100% |
E9AU50 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 63% | 100% |
Q4Q0E5 | Leishmania major | 64% | 99% |